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Pharmacovigilance Coordinator

Propharma
1+ years
4.5 LPA - 17.5 LPA
Remote, India, India
1 June 30, 2026
Job Description
Job Type: Hybrid Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: ICH guidelines, ICSR Case Processing, Labelling Assessment, MedDRA Coding, mRS and EQ-5D-5L, Triage of ICSRs, WHO DD Coding

Pharmacovigilance Coordinator

Company: ProPharma
Location: India
Department: Pharmacovigilance / Drug Safety
Job Type: Full-Time
Work Mode: Remote / Hybrid (Based on Location)

JOB OVERVIEW

The Pharmacovigilance Coordinator is responsible for supporting pharmacovigilance operations by managing safety communications, processing adverse event reports, performing duplicate searches, screening source documents, conducting literature surveillance activities, and maintaining accurate safety database records. The role involves case intake, data entry, regulatory database review, client communication, documentation management, and ensuring compliance with global pharmacovigilance regulations and company procedures.


KEY RESPONSIBILITIES

Safety Case Intake & Processing

  • Manage assigned pharmacovigilance mailboxes and client communications.

  • Perform initial case intake and book-in activities.

  • Conduct duplicate searches for incoming safety cases.

  • Process inbound adverse event reports accurately.

  • Support end-to-end safety case management activities.

Safety Database Management

  • Enter essential safety information into pharmacovigilance databases.

  • Record patient, reporter, suspect drug, and adverse event details.

  • Perform complete case data entry when qualified and trained.

  • Maintain accurate and timely safety records.

  • Ensure data quality and database integrity.

Literature & Regulatory Surveillance

  • Support literature surveillance activities.

  • Perform initial triage of regulatory authority database searches.

  • Review literature findings for potential safety information.

  • Assist in identifying reportable safety cases.

  • Maintain documentation of literature review activities.

Documentation & Privacy Compliance

  • Screen and redact Protected Health Information (PHI) from source documents.

  • Ensure compliance with company privacy procedures.

  • Maintain complete and accurate case documentation.

  • Follow pharmacovigilance SOPs and regulatory requirements.

  • Support inspection-ready documentation practices.

Client Communication

  • Manage client-related pharmacovigilance communications.

  • Send draft reports to clients for review when required.

  • Coordinate internal and external case-related communications.

  • Maintain timely communication with stakeholders.

  • Support client-specific pharmacovigilance processes.

Operational Support

  • Prioritize multiple pharmacovigilance tasks efficiently.

  • Collaborate with cross-functional pharmacovigilance teams.

  • Maintain high-quality documentation standards.

  • Support continuous improvement initiatives.

  • Perform additional pharmacovigilance duties as assigned.


EDUCATIONAL QUALIFICATIONS

Required

Post-Secondary Education in:

  • Pharmacy

  • Life Sciences

  • Biotechnology

  • Biomedical Sciences

  • Nursing

  • Healthcare

  • Or a related discipline


EXPERIENCE REQUIREMENTS

Preferred

  • Minimum 1 year of experience in:

    • Pharmacovigilance

    • Drug Safety

    • Clinical Research

    • Healthcare

    • Pharmaceutical Industry

Preferred Experience

  • Safety case intake and processing.

  • Pharmacovigilance database entry.

  • Literature surveillance.

  • Duplicate search activities.

  • Adverse event documentation.

  • Client communication.

  • PHI redaction and privacy compliance.

  • Regulatory database review.